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http://rdf.disgenet.org/nanopublications.trig#NP762104.RAcAh4dHaU254StH8SfoiASD7lDJP_xp867ollkqREDac
> .
@prefix rdfs: <
http://www.w3.org/2000/01/rdf-schema#
> .
@prefix xsd: <
http://www.w3.org/2001/XMLSchema#
> .
@prefix sio: <
http://semanticscience.org/resource/
> .
@prefix ncit: <
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#
> .
@prefix lld: <
http://linkedlifedata.com/resource/umls/id/
> .
@prefix miriam-gene: <
http://identifiers.org/ncbigene/
> .
@prefix miriam-pubmed: <
http://identifiers.org/pubmed/
> .
@prefix eco: <
http://purl.obolibrary.org/obo/eco.owl#
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/2.0/
> .
@prefix prv: <
http://purl.org/net/provenance/ns#
> .
@prefix dcterms: <
http://purl.org/dc/terms/
> .
@prefix np: <
http://www.nanopub.org/nschema#
> .
@prefix dgn-np: <
http://rdf.disgenet.org/nanopublications.trig#
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/gene-disease-association.ttl#
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
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{
this:
np:hasAssertion
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;
np:hasProvenance
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;
np:hasPublicationInfo
dgn-np:NP762104.RAcAh4dHaU254StH8SfoiASD7lDJP_xp867ollkqREDac130_publicationInfo
;
a
np:Nanopublication
.
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a
np:Assertion
.
dgn-np:NP762104.RAcAh4dHaU254StH8SfoiASD7lDJP_xp867ollkqREDac130_provenance
a
np:Provenance
.
dgn-np:NP762104.RAcAh4dHaU254StH8SfoiASD7lDJP_xp867ollkqREDac130_publicationInfo
a
np:PublicationInfo
.
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{
miriam-gene:1277
a
ncit:C16612
.
lld:C0013720
a
ncit:C7057
.
dgn-gda:DGNdad2b1f4463c7b592f564db8874b8fac
sio:SIO_000628
miriam-gene:1277
,
lld:C0013720
;
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.
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dgn-np:NP762104.RAcAh4dHaU254StH8SfoiASD7lDJP_xp867ollkqREDac130_provenance
{
dgn-np:NP762104.RAcAh4dHaU254StH8SfoiASD7lDJP_xp867ollkqREDac130_assertion
dcterms:description
"[Thus, in contrast to mutations in genes that encode the dominant protein of a tissue (e.g., COL1A1 and COL2A1), in which `null` mutations result in phenotypes milder than those caused by mutations that alter protein sequence, the phenotypes produced by these mutations in COL3A1 overlap with those of the vascular form of EDS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
;
sio:SIO_000772
miriam-pubmed:11577371
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20140225
pav:importedOn
"2014-02-25"^^
xsd:date
.
dgn-void:source_evidence_literature
a
eco:ECO_0000212
;
rdfs:comment
"Gene-disease associations inferred from text-mining the literature."@en ;
rdfs:label
"DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP762104.RAcAh4dHaU254StH8SfoiASD7lDJP_xp867ollkqREDac130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:41+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
;
dcterms:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
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pav:authoredBy
<
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> , <
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> , <
http://orcid.org/0000-0002-9383-528X
> , <
http://orcid.org/0000-0003-0169-8159
> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
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